codman eds 3 external drainage system
TRANSCRIPT
integralife.euA D I V I S I O N O F I N T E G R A L I F E S C I E N C E S
For an easy-to-use solution, choose the
• Entirely disposable, complete system
• Simple set up
• Laser accuracy
• Needle-free access
• Latex & PVC free
Codman® EDS 3™ EXTERNAL DRAINAGE SYSTEM
The Codman® EDS 3™ External
Drainage System was developed
with input from more than 200
nurses and physicians.
Drip Chamber with hydrophobic & haemorepellent filter marked for 0-100ml capacity, funnel bottom, and sampling site (outlet)
Pressure-resistant striped CSF tubing line
Redesigned drainage bag with needle-free access port
Improved, larger tubing connecting the drip chamber and the drainage bag
Reusable Leveling Device incorporates bubble level with laser lamp
High-visibility pressure scales in mmHg (-3 to 20) and cmH2O (-5 to 27)
Codman® VersaTru® Disposable Non-Stick Bipolar ForcepsYour Partner in Challenging Situations
3
CSF EXTERNAL DRAINAGE SYSTEM DESIGNED WITH AND FOR CLINICIANS
Easy Setup
6 Adjust drip chamber height until black level is at the proper drainage resistance pressure with White Screw.
4 Push to engage the laser.
5 Adjust system height on the I.V. pole for proper zero reference with Blue Screw.
3 Level to the floor with Black Screw.
2 Insert Leveling Device.
1 Attach system to I.V. pole with Blue Screw.
Purchase our BACTISEAL® EVD Catheter with the Codman® EDS 3™ System.
If any part of the system requires a revision due to infection or component failure,
Codman Specialty Surgical will replace those components free of charge.
OUR PLEDGE TO YOU BACTISEAL EVD + EDS 3 = CONFIDENCE
Integra LifeSciences Services (France) SAS Immeuble Séquoia 2 97 allée Alexandre Borodine Parc technologique de la Porte des Alpes 69800 Saint Priest n France Phone: +33 (0)4 37 47 59 00 n +33 (0)4 37 47 59 99 (fax) integralife.eu
Sales & Marketing EMEA
Customer services EMEA Europe, Middle-East, Africa: +33 (0)4 37 47 59 50 n +33 (0)4 37 47 59 25 (Fax) n [email protected] France: +33 (0) 437 47 59 10 n +33 (0) 437 47 59 29 (Fax) n [email protected] Benelux: +32 (0)2 257 4130 n +32 (0)2 253 2466 (Fax) n [email protected] Germany: +49 (0) 2102 5535 6200 n +49 (0)2 102 553 6636 (fax) n [email protected] Italy : +39 (0)2 577 89 21 n +39 (0)2 575 113 71 n [email protected] Switzerland: +41 (0)2 27 21 23 30 n +41 (0)2 27 21 23 99 (Fax) n [email protected] United Kingdom: +44 (0)1264 312 725 n +44 (0)1264 312 821 (fax) n [email protected]
Integra LifeSciences Services (France) Immeuble Séquoïa 297 Allée Alexandre BorodineParc Technologique de la Porte des Alpes69800 Saint Priest i France
Integra LifeSciences Production Corporation11 Cabot BoulevardMansfield i MA 02048 i USA
Availability of these products might vary from a given country or region to another, as a result of specific local regulatory approval or clearance requirements for sale in such country or region. n Non contractual document. The manufacturer reserves the right, without prior notice, to modify the products in order to improve their quality. n Warning: Applicable laws restrict these products to sale by or on the order of a physician. n Consult product labels and inserts for any indication, contraindications, hazards, warnings, precautions, and instructions for use.
Products mentioned in this document are CE risk class I and III devices. Please contact Integra customer service should you need any additional information on devices classification. All the medical devices mentioned on this document are CE marked in accordance with the applicable European laws, unless specifically identified as “NOT CE MARKED”.
Bactiseal, EDS 3C, Codman, Integra, and the Integra logo are registered trademarks of Integra LifeSciences Corporation or its subsidiaries in the United States and/or other countries. ©2021 Integra LifeSciences Corporation. All rights reserved. Last revision date: 08/2021. 1012252-3-ENDOCUMENT FOR USE IN EUROPE, MIDDLE-EAST and AFRICA.
1.Ingraham FD and Campbell JB: An apparatus for closed drainage of the ventricular system. Ann Surg 114: 1096–1098, 19412. Bering EA: A simplified apparatus for constant ventricular drainage. J Neurosurg 8: 450–452, 1951.3. White RJ, Dakters J, Young H, et al: continuous control of CSF volume and pressure with an externalized valve-drainage system. Trans Am Soc Artif Intern Organs 13: 332–333, 1967.4. White RK, Dakters JG, et al: Temporary control of cerebrospinal fluid volume and pressure by means of an externalized valve-drainage system. J Neurosurg 30: 264–269, 1969.
Confidence in providing a TOTAL DRAINAGE SOLUTION
PART NO. DESCRIPTION
821745
1.5mm Inner Lumen Diameter
821749
1.9mm Inner Lumen Diameter
821750
1.9mm Clear Inner Lumen Diameter
PART NO. DESCRIPTION
821730CCodman® External Drainage System EDS 3™ with ventricular catheter
821731CCODMAN® External Drainage System EDS 3™ No Ventricular Catheter
821732C EDS 3™ Collection Bag Kit - 5 Bags
821733 EDS 3™ Leveling Device
IndicationsThe Codman® BACTISEAL® EVD Catheter and Codman® BACTISEAL® Clear EVD Catheter Sets (BACTISEAL® EVD Catheters), are indicated for gaining access to the ventricles of the brain and can be used with dimensionally compatible devices for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means of reducing intracranial pressure and CSF volume.Use of the Codman® EDS 3™ CSF External Drainage System (EDS 3) is indicated for draining cerebrospinal fluid (CSF) and other fluids of similar physical characteristics as a means of reducing intracranial pressure and CSF volume. 1–4ContraindicationsCodman® EDS 3™: Use of this device is contraindicated if scalp infection is present. Use of this device is contraindicated for patients receiving anticoagulants or for patients who are known to have a bleeding diathesis. Use of this device is contraindicated where 24-hour supervision from trained personnel is not available.Bactiseal®: Do not implant this device in patients with active infections, such as ventriculitis meningitis, or skin infections at or near the implantation site. Treat the infection before implanting this device. Do not implant this device in patients with known hypersensitivity to rifampin or clindamycin hydrochloride. Use of this device is contraindicated in patients receiving anticoagulants or known to have a bleeding diasthesis.